© 2015, Science Press. All right reserved. Microbial electrolysis cells (MECs) has been recently developed as a new technology for hydrogen production. The organics are degraded by exoelectrogens in anode biofilm and transport electrons directly to anode, while hydrogen is produced by combining electrons and protons on the surface of Pt-catalyzing cathode under a small external voltage between anode and cathode. Municipal waste water was used as the same inoculum to enrich functional communities in 15 single chamber MEC reactors. Various gas production (hydrogen and methane) was maintained over 1 month using glucose as the sole carbon source in phosphate buffer solution (50 mmol·L-1, pH=7.0). The highest hydrogen production rate was up to (3.9±0.6) mol H2/mol glucose with conversion rate of 32.2% for high-H2generation MECs. The highest methane conversion rate was 48.4% in low-H2generation MECs. A 48 h low pH shock was put into anode biofilm and MEC performances were recovered to their functions in 10~15 d. The microbial diversities increased and gas production rates were changed after low pH shock. Hydrogen yield was reduced by 1.8 mol H2/mol glucose in high-H2generation MECs, while the methane yield increased by 0.4 mol CH4/mol glucose. Based on Geochip analysis, cytochrome C genes were mostly enriched in high-H2yield MECs. Thus functional genes were still recovered dominantly after low pH shock and it supported the recovery of electron transport. The carbon degradation genes were substantially changed among anodic communities in most MECs. The functional genes of labile carbon degradation and methane production were significantly changed after microbial community recovery. The carbon degradation gene structure was more significantly changed in high-H2yield MECs than high-methane yield MECs. The methane increase and hydrogen decrease matched well with their stoichiometric relationship.

Background Retropharyngeal metastases are uncommon but a well-known location for regional spread of well-differentiated thyroid carcinoma (WDTC). Surgeon-performed, trans-oral ultrasound (SP-TO-US) and trans-oral robot-assisted surgical (TORS) excision represent a unique combination of technology and techniques in the treatment of isolated retropharyngeal thyroid metastases. Patient findings A patient with a history of T3N1b papillary thyroid carcinoma (PTC) previously treated with total thyroidectomy, left central and lateral neck dissection, and radioactive iodine presented with progressive elevations in serum thyroglobulin (Tg) from baseline of 0.2 to 0.6 μg/L. She was found to have an isolated 2.6 cm left retropharyngeal nodal metastasis on MRI that was confirmed to be PTC on fine needle aspiration biopsy. She underwent SP-TO-US for identification of the node in the operating room immediately prior to TORS excision. There were no complications. Additional radioactive iodine was administered. Post-treatment iodine scans revealed resolution of avid uptake in left retropharynx and return of Tg to 0.2 μg/L. Summary The combination of SP-TO-US and TORS represents a novel combination of technology and technique for treatment of isolated retropharyngeal metastasis in WDTC. Trans-oral ultrasound allows for rapid localization of the lesion in relation to the adjacent neurovascular structures in the parapharynx while the robot-assisted approach affords a safe and effective dissection through the improved visualization and dexterity in a small working space. Our patient had no complications and only short-term dysphagia that resolved after temporary diet alteration. Risks and long-term morbidities associated with classical approaches to the retropharynx including trans-cervical and trans-mandibular, particularly in a previously dissected field, are avoided through this trans-oral approach. Conclusions Retropharyngeal metastases are a known location for regional spread of WDTC and are amenable to evaluation and biopsy using TO-US by both surgical and non-surgical providers. In cases where lateral neck dissection has already been performed or when traditional transcervical or transmandibular approaches to the retropharynx represent a comparatively extensive procedure for isolated metastases, SP-TO-US and TORS are safe and effective combination for surgical management of disease.

An experimental study of software image compositing that we have carried out on a 512-node PC cluster shows the necessity of hardware compositing support to make possible real-time volume visualization scalable with large PC clusters. This paper describes the design and performance evaluation of such a hardware image compositing device. A PC cluster using such devices along with commodity graphics cards can enable simultaneous simulation and volume visualization.

We previously demonstrated that the organophosphate diisopropylfluorophosphate (DFP) induced region-specific delayed neuronal injury in rat brain. The goal of this study was to examine the spatiotemporal pattern of the astroglial response after acute intoxication of rats with DFP. Rats were euthanized at varying times between 1 h to 7 days after DFP administration (9mg/kg, i.p.). The distribution of activated astrocytes in different brain regions was determined by immunostaining for glial fibrillary acidic acid (GFAP). GFAP immunoreactivity increased in the hippocampus, and piriform/entorhinal cortex at 1 h, peaked between 4-8 h then decreased from 16 to 24 h. GFAP labeling in the amygdala gradually increased over the 24 h period. A large increase in GFAP labeling was seen at 3-7 days following DFP administration in the hippocampus, piriform/entorhinal cortex and dorsolateral thalamus. At 3 days post-DFP exposure, GFAP immunoreactivity was totally absent in central areas of the hippocampus, piriform/entorhinal cortex and dorsolateral thalamus that contained numerous FluoroJade B (FJB) labeled neurons. By 7 days, GFAP expression was highly upregulated in all areas of each brain region. The mRNA expression of GFAP in hippocampus slowly increased at 24 h following DFP administration then dramatically increased at 3 days. This study suggests that activation of glial cells may contribute to the early neuropathological changes and later neuronal repair/plasticity following acute DFP intoxication.

Persistent currents in superconducting magnet introduce magnetic errors especially at low operating fields. In addition, their decay causes magnetic field variations and therefore drifts of the beam orbits, tunes, and chromaticities. To reduce field errors and suppress magnetic field variations, a new magnetic cycle was proposed for the low-energy beam operation at the Relativistic Heavy Ion Collider (RHIC). In the new magnetic cycle, the magnet current oscillates around the nominal operating current with diminishing amplitude a few times before it settles. The new magnetic cycle has been demonstrated experimentally to reduce field errors and the amplitude of magnetic field variations significantly and is essential for the ongoing RHIC Beam Energy Scan II (BES-II) program. This article will present beam-based experimental studies of the persistent current effects with the new magnetic cycle, and discuss its application in RHIC.

Decision making ability has been reported to be impaired in schizophrenia patients, but no research has examined the genetic bases of this impairment. This study investigated how decision making was affected by the genetic variants in the serotonin transporter gene (triallelic 5- HTTLPR) and serotonin receptor 1A gene (rs6295) and their interaction in 465 schizophrenia patients and 448 healthy controls. The Iowa Gambling Task (IGT) was used to evaluate decision making under ambiguity (the first 40 trials) and decision making under risk (the last 60 trials). Results showed that, among the patients, the main effects of 5- HTTLPR (F(2) (,16) = 6.54, P = 0.002) and HTR1A rs6295 (F(2) (,16) = 3.87, P = 0.021) polymorphisms and their interaction effect (F(4) (,16) = 3.32, P = 0.005) were significant for the first 40 trials, with the GG genotype of HTR1A rs6295, the L'L' genotype of 5- HTTLPR and the GG-L'L' combination showing poorer IGT performance than their counterparts. Results for the healthy controls showed a similar pattern but did not reach statistical significance. No significant effects were found for the last 60 trials. These results are discussed in terms of their implications for our understanding of the genetic mechanisms of decision making in schizophrenia patients as well as healthy adults.